9IUT
Crystal structure of cancer-specific anti-HER2 antibody H2Mab-250 in complex with epitope peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL44XU |
Synchrotron site | SPring-8 |
Beamline | BL44XU |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2021-05-14 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 116.545, 123.199, 96.083 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 37.070 - 2.090 |
R-factor | 0.203 |
Rwork | 0.201 |
R-free | 0.23580 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.002 |
RMSD bond angle | 0.554 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.19.2_4158) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.300 | 2.220 |
High resolution limit [Å] | 2.090 | 2.090 |
Number of reflections | 41195 | 6539 |
<I/σ(I)> | 10.66 | 2.08 |
Completeness [%] | 99.8 | 99.2 |
Redundancy | 6.7 | 6.5 |
CC(1/2) | 0.997 | 0.798 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 293 | 0.2 M MgCl2, 0.1 M Bis-Tris pH 5.7, 25% w/v PEG 3350 |